North Woods Derma Foam Hand Sanitizer

Manufacturer: Superior Chemical Corporation | Betco corporation, Ltd.
Effective date: 2019-04-09
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-05-31 22:59:07

Label at a glance#

ProductNorth Woods Derma Foam Hand Sanitizer

Active ingredientBENZALKONIUM CHLORIDE

Label structure9 sections

Contacts and useful links#

PhoneLabel contact(800) 777-9343

PhoneLabel contact(800) 891-4965

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient

Benzalkonium Chloride 0.13%

INDICATIONS & USAGE SECTION

Uses

Use in a variety of public facilities.
Use this product when soap and water are not available.

WARNINGS SECTION

Warnings

For external use only.
Avoid contact with eyes.
Children under the age of 6 should be supervised by an adult when using this product.
Discontinue use is irritation or redness develops.
If irritation persists for more than 72 hours, consult a physician.
KEEP OUT OF REACH OF CHILDREN.

DOSAGE & ADMINISTRATION SECTION

Directions

Read the entire label before using this product.
Dispense product onto dry hands. Rub hands together until hands are dry.
Use as needed between hand washes to reduce bacteria on the skin.

INACTIVE INGREDIENT SECTION

Inactive Ingredients

Deionized Water, Sodium PCA, PEG/PPG-8/3 Laurate, Dimethicone, DMDM Hydantoin, PEG-3 Cocamide, Fragrance, Iodoproynyl Btylcarbamate, D&C Green #5.

OTC - QUESTIONS SECTION

Questions or Comments?Phone: (800) 777-9343

MDS information:(800) 891-4965

OTC - PURPOSE SECTION

Purpose

Antiseptic

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN

Superior Derma Foam Hand Sanitizer

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

75229-00_Superior Derma Foam Hand Sanitizer. 75229 Superior Derma Foam

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1020365	benzalkonium chloride 0.13 % Topical Foam	PSN	2
1020365	benzalkonium chloride 1.3 MG/ML Topical Foam	SCD	2
1020365	benzalkonium chloride 0.13 % Topical Foam	SY	2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
53125-700-54	2024-10-01	C162847	48780-1	1030e365-3c5a-111a-e063-dadaa90a10e2	North Woods Derma Foam Hand Sanitizer
53125-700-57	2024-10-01	C162847	48780-1	1030e365-3c5a-111a-e063-dadaa90a10e2	North Woods Derma Foam Hand Sanitizer
53125-700-54	2024-07-30	C162847	48780-1	1030e365-3c5a-111a-e063-dadaa90a10e2	North Woods Derma Foam Hand Sanitizer
53125-700-57	2024-07-30	C162847	48780-1	1030e365-3c5a-111a-e063-dadaa90a10e2	North Woods Derma Foam Hand Sanitizer
53125-700-54	2024-01-30	C162847	48780-1	1030e365-3c5a-111a-e063-dadaa90a10e2	North Woods Derma Foam Hand Sanitizer
53125-700-57	2024-01-30	C162847	48780-1	1030e365-3c5a-111a-e063-dadaa90a10e2	North Woods Derma Foam Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
53125-700-54	North Woods Derma Foam Hand Sanitizer	1000 mL in 1 BAG	SOAP	1000		2
53125-700-57	North Woods Derma Foam Hand Sanitizer	550 mL in 1 BOTTLE, PUMP	SOAP	550		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
53125-700	NORTH WOODS DERMA FOAM HAND SANITIZER (BENZALKONIUM CHLORIDE) SOAP [SUPERIOR CHEMICAL CORPORATION]	2	Current NDC, Legacy NDC, 2 package rows	20190410_861e2386-96cf-8b8e-e053-2991aa0ac57a.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 11 matching rows.

North Woods Derma Foam Hand Sanitizer
Benzalkonium Chloride
WATER
SODIUM PYRROLIDONE CARBOXYLATE
POLYETHYLENE GLYCOL 400
DIMETHICONE
DMDM HYDANTOIN
PEG-3 COCAMINE
IODOPROPYNYL BUTYLCARBAMATE
D&C GREEN NO. 5
BENZALKONIUM

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
53125-700	53125-700-57, 53125-700-54

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
SODIUM PYRROLIDONE CARBOXYLATE	469OTG57A2	IACT
POLYETHYLENE GLYCOL 400	B697894SGQ	IACT
DIMETHICONE	92RU3N3Y1O	IACT
DMDM HYDANTOIN	BYR0546TOW	IACT
PEG-3 COCAMINE	KTM00873VC	IACT
IODOPROPYNYL BUTYLCARBAMATE	603P14DHEB	IACT
D&C GREEN NO. 5	8J6RDU8L9X	IACT
BENZALKONIUM CHLORIDE	F5UM2KM3W7	ACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 2 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
North Woods Derma Foam Hand Sanitizer	BENZALKONIUM CHLORIDE	Superior Chemical Corporation	ad51a175-2b91-fd14-e053-2995a90ad54d	2026-09-09	Warnings	Exact identifier ndc (product): 53125-700
861e2386-96d0-8b8e-e053-2991aa0ac57a			861e2386-96cf-8b8e-e053-2991aa0ac57a	2019-04-09	Warnings	Exact identifier spl id: 861e2386-96d0-8b8e-e053-2991aa0ac57a spl set id: 861e2386-96cf-8b8e-e053-2991aa0ac57a

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.